Canadian Journal of Chemistry · 1984 · 63 citations · 5 references
Life SciencesBiochemistryMedicinal ChemistryEnzymologyMolecular VirologyVirologyAntiviral PharmacologyAntiviral TherapyNucleic Acid SynthesisNucleotide MetabolismPhosphodiester Bond ChemistryAntiviral Structure-activity RelationshipsNucleoside AnalogsNucleoside Analogue AntiviralsPurine AnaloguesPurine Degradation
The synthesis of a series of purine analogues of the acyclonucleoside compound A* (A-Star, 1) is described. Compounds in this series have been shown to have pronounced activity against herpesviruses. These compounds have been designated "the glycerosides". The glyceropurines are described in this report. Nucleotides have been constructed containing glyceroadenine (A*, compound 1). These nucleotides are resistant to degradation by phosphodiesterases. The compound A* is both a poor substrate and a poor inhibitor of adenosine deaminase.
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N-Substituted Acyclopurinenucleosides with Antiviral Activity
Kelvin K. Ogilvie, H. R. Hanna, Nghe Nguyen‐Ba et al. · Nucleosides and Nucleotides · 1985 · 12 citations